Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.78625057A>GCA7684689CHRNB4c.*76T>C (n.*76T>C)
c.594T>C (p.Ala198=)
c.777T>C (p.Ala259=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.78625057A>TCA715980697CHRNB4c.*76T>A (n.*76T>A)
c.594T>A (p.Ala198=)
c.777T>A (p.Ala259=)
dbSNP gnomAD v4

Number of alleles fetched